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Thomas Sejersen Department of Women´s and Children´s Health, Karolinska Institutet, S-17176 StockholmSweden
Case Report Spg3a Mutation Co-Segregates with Hereditary Spastic Paraplegia Phenotype Whereas SPG31 Duplication Does Not Author(s): Thomas Sejersen and Shera GustafssonThomas Sejersen and Shera Gustafsson
DOI: 10.4172/2155-9562.1000129
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